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Bárbara L. T. Rosa

Publications and source records attributed to Bárbara L. T. Rosa.

4 recordsLinked to original sources

An integrated all-van der Waals nanobeam laser

Transition-metal dichalcogenides offer a promising platform for integrated coherent light sources, yet lasing has largely relied on hybrid photonic architectures without direct quantum-optical verification. Here, we demonstrate an all-van der Waals (all-vdW) high-$β$ nanobeam laser based on a WS$_2$/MoSe$_2$/WS$_{2}$ heterostructure, with the MoSe$_2$ monolayer directly integrated in the WS$_{2}$-based optical resonator for optimal gain-mode overlap. The devices exhibit efficient exciton-cavity coupling at cryogenic temperatures, strongly directional and linearly polarized emission, soft nonlinear input-output characteristics and linewidth narrowing, enabling lasing operation with $β$ near unity. Excitation-power-dependent photon-autocorrelation measurements reveal a transition from thermal to Poissonian photon statistics, with $g_{\mathrm{peak}}^{(2)}(0)$ decreasing from $(1.28\,\pm\,0.09)$ near threshold to $(1.07\,\pm\,0.07)$ above threshold, directly verifying lasing operation. Furthermore, temporal broadening of the autocorrelation uncovers fluctuation-dominated lasing dynamics. These results establish all-vdW heterostructures as a highly attractive platform for integrated coherent light sources in layered-material photonic architectures and scalable quantum-photonic circuits.

physics.optics↗

Probing Interface-Driven Mechanisms of Non-Classical Light in van der Waals Heterostructures

Single-photon emitters in two-dimensional semiconductors offer a versatile platform for integrated quantum photonics, yet their performance is strongly influenced by local dielectric environments and substrate-induced disorder. Here, we examine SPEs in monolayer WSe$_2$ incorporated into hBN/WSe$_2$/Clinochlore van der Waals heterostructures and assess how interface-mediated dielectric modulation governs their optical and quantum characteristics. Low-temperature micro-photoluminescence reveals narrow emission lines (100 - 300 $μ$eV) and robust non-classical behavior, with $g^{(2)}(0) = 0.13 \pm 0.02$ on SiO$_2$ and $0.54 \pm 0.02$ for emitters directly coupled to Clinochlore. Magneto-optical measurements yield effective g-factors near -8, consistent with defect states hybridized with dark excitons. WSe$_2$ on Clinochlore exhibits up to a fivefold enhancement in emission intensity, attributed to coupling with Fe-related substrate states that introduce resonant absorption near 1.75 eV. Kelvin probe force microscopy confirms strong dielectric contrast across thin and thick Clinochlore regions. Time-resolved photoluminescence shows that emitters on SiO$_2$ display a single $\approx 4$ ns lifetime, whereas those on Clinochlore exhibit biexponential dynamics with sub-nanosecond and tens-of-nanoseconds decay components. A phenomenological model incorporating coupling to bright and dark Fe-related states in Clinochlore accounts for modified excitation pathways. These results establish interface dielectric engineering in vdW heterostructures as an effective strategy for tailoring the radiative dynamics and brightness of quantum emitters in atomically thin materials.

cond-mat.mtrl-sci↗

Electrical manipulation of intervalley trions in twisted MoSe$_2$ homobilayers at room temperature

The impressive physics and applications of intra- and interlayer excitons in a transition metal dichalcogenide twisted-bilayer make these systems compelling platforms for exploring the manipulation of their optoelectronic properties through electrical fields. This work studies the electrical control of excitonic complexes in twisted MoSe$_2$ homobilayer devices at room temperature. Gate-dependent micro-photoluminescence spectroscopy reveals an energy tunability of several meVs originating from the emission of excitonic complexes. Furthermore, our study investigates the twist-angle dependence of valley properties by fabricating devices with stacking angles of $θ\sim1\degree$, $θ\sim4\degree$ and $θ\sim18\degree$. Strengthened by density functional theory calculations, the results suggest that, depending on the twist angle, the conduction band minima and hybridized states at the \textbf{Q}-point promote the formation of intervalley hybrid trions involving the \textbf{Q}-and \textbf{K}-points in the conduction band and the \textbf{K}-point in the valence band. By revealing the gate control of exciton species in twisted homobilayers, our findings open new avenues for engineering multifunctional optoelectronic devices based on ultrathin semiconducting systems.

cond-mat.mtrl-sci↗

Nature of long-lived moiré interlayer excitons in electrically tunable MoS$_{2}$/MoSe$_{2}$ heterobilayers

Interlayer excitons in transition-metal dichalcogenide heterobilayers combine high binding energy and valley-contrasting physics with long optical lifetime and strong dipolar character. Their permanent electric dipole enables electric-field control of emission energy, lifetime, and location. Device material and geometry impacts the nature of the interlayer excitons via their real- and momentum-space configurations. Here, we show that interlayer excitons in MoS$_{2}$/MoSe$_{2}$ heterobilayers are formed by charge carriers residing at the Brillouin zone edges, with negligible interlayer hybridization. We find that the moiré superlattice leads to the reversal of the valley-dependent optical selection rules, yielding a positively valued g-factor and cross-polarized photoluminescence. Time-resolved photoluminescence measurements reveal that the interlayer exciton population retains the optically induced valley polarization throughout its microsecond-long lifetime. The combination of long optical lifetime and valley polarization retention makes MoS$_{2}$/MoSe$_{2}$ heterobilayers a promising platform for studying fundamental bosonic interactions and developing excitonic circuits for optical information processing.

cond-mat.mes-hall↗